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Protein Coding Gene : Exosc9 exosome component 9

Primary Identifier  MGI:1355319 Organism  mouse, laboratory
Chromosome  3 NCBI Gene Number  50911
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable RNA polymerase II-specific DNA-binding transcription factor binding activity and mRNA 3'-UTR AU-rich region binding activity. Predicted to be involved in RNA metabolic process; positive regulation of cell growth; and positive regulation of transcription by RNA polymerase II. Predicted to act upstream of or within rRNA processing. Predicted to be located in cytosol and nuclear lumen. Predicted to be part of cytoplasmic exosome (RNase complex) and nuclear exosome (RNase complex). Is expressed in several structures, including cerebral cortex; gonad; liver; metanephros; and muscle tissue. Human ortholog(s) of this gene implicated in pontocerebellar hypoplasia type 1D. Orthologous to human EXOSC9 (exosome component 9).
  • synonyms:
  • Pmscl1,
  • Exosc9,
  • exosome component 9,
  • p6,
  • p5,
  • PM/Scl-75,
  • polymyositis/scleroderma autoantigen 1,
  • RRP45

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

2 Involved In Mutations

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

10 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For